Table 2.
Surgical and perioperative characteristics of infants enrolled in the NITric oxide during cardiopulmonary bypass to improve Recovery in Infants with Congenital heart defects (NITRIC) trial
| Characteristics | Nitric oxide N = | Standard care N = | Difference (95% CI) |
|---|---|---|---|
| Cardiopulmonary bypass characteristics | |||
| Blood prime, n (%) | |||
| CPB duration (min), median (IQR) | |||
| CPB < 60 min, n (%) | |||
| CPB ≥ 60 min, n (%) | |||
| Cross-clamp, n (%) | |||
| Cross-clamp (min), median (IQR) | |||
| Number of CPB runs, n (%) | |||
| 1 | |||
| 2 | |||
| 3 | |||
| ≥ 4 | |||
| Deep hypothermic arrest, n (%) | |||
| Duration of deep hypothermic arrest (min), median (IQR) | |||
| Antegrade cerebral perfusion, n (%) | |||
| Modified ultrafiltration used, n (%) | |||
| Slow continuous ultrafiltration used, n (%) | |||
| Blood products received in theatre, median (IQR) | |||
| Red blood cells (mL/kg) | |||
| Whole blood (mL/kg) | |||
| Platelets (mL/kg) | |||
| Fresh frozen plasma (mL/kg) | |||
| Cryoprecipitate (mL/kg) | |||
| Drug treatments received in theatre, n (%) | |||
| Intravenous steroids | |||
| Inhaled NO | |||
| Administration of study drug (NO) | |||
| Time from start of CPB to start of NO (min), mean (SD)/median (IQR) | |||
| Duration of NO on CPB (min), median (IQR) | |||
| Proportion of time spent on CPB with NO,⁎ mean (SD)/median (IQR) | |||
| Change in methaemoglobin level (%) between start and post-CPB, mean (SD)/median (IQR)† | |||
| Change in methaemoglobin level (%) between start and post-CPB > 3%,†n (%) |
CPB = cardiopulmonary bypass; IQR = interquartile range; NO = nitric oxide; SD = standard deviation.
If multiple CPB runs during the same surgery, summarising every CPB run individually.
Calculated as post-CPB methaemoglobin/pre-CPB methaemoglobin.